GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 7076 - 7100 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism
DOID:1612
  • breast cancer
  • Aliases:
    • breast tumor
    • malignant neoplasm of breast
    • malignant tumor of the breast
    • mammary cancer
    • mammary tumor
    • primary breast cancer
Mus musculus (house mouse)
DOID:557
  • kidney disease
  • Aliases:
    • impaired renal function disease
    • nephropathy
Rattus norvegicus (Norway rat)
DOID:0050526
  • Gamstorp-Wohlfart syndrome
  • Aliases:
    • autosomal recessive neuromyotonia and axonal neuropathy
    • myokymia, myotonia and muscle wasting
Homo sapiens (human)
DOID:684
  • hepatocellular carcinoma
  • Aliases:
    • Hepatoma
Xenopus laevis (African clawed frog)
DOID:0110569
  • autosomal dominant nonsyndromic deafness 44
  • Aliases:
    • DFNA44
    • autosomal dominant deafness 44
Homo sapiens (human)
DOID:3827
  • congenital diaphragmatic hernia
  • Aliases:
    • Diaphragmatic Hernia
Drosophila melanogaster (fruit fly)
DOID:12858
  • Huntington's disease
  • Aliases:
    • HD
    • Huntington disease
    • Huntington's chorea
Danio rerio (zebrafish)
DOID:0080558
  • congenital disorder of glycosylation If
  • Aliases:
    • congenital disorder of glycosylation 1f
Mus musculus (house mouse)
DOID:891
  • progressive myoclonus epilepsy
  • Aliases:
    • PME
    • progressive myoclonic epilepsy
Homo sapiens (human)
DOID:0070253
  • congenital disorder of glycosylation type IIa
  • Aliases:
    • Alkuraya syndrome
    • CDG IIa
    • CDG2A
    • CDGIIa
    • CDGS2
    • carbohydrate-deficient glycoprotein syndrome, type II
    • congenital disorder of glycosylation, type IIa
    • mental retardation, growth retardation, prominent columella, and open mouth
Caenorhabditis elegans
DOID:0110461
  • X-linked dilated cardiomyopathy
  • Aliases:
    • CMD3B
    • DMD-related dilated cardiomyopathy
Homo sapiens (human)
DOID:10457
  • Legionnaires' disease
  • Aliases:
    • Infection by Legionella pneumophilia
    • Legionella
    • Legionella pneumonia
    • Legionnaire's disease
Drosophila melanogaster (fruit fly)
DOID:8632
  • Kaposi's sarcoma
  • Aliases:
    • Kaposi sarcoma
    • Kaposi's sarcoma of Heart
    • Kaposi's sarcoma of anus
    • Kaposi's sarcoma of central nervous system
    • Kaposi's sarcoma of conjunctiva
    • Kaposi's sarcoma of cornea
    • Kaposi's sarcoma of esophagus
    • Kaposi's sarcoma of gastrointestinal sites
    • Kaposi's sarcoma of lung
    • Kaposi's sarcoma of lymph nodes
    • Kaposi's sarcoma of palate
    • Kaposi's sarcoma of penis
    • Kaposi's sarcoma of skin
    • Kaposi's sarcoma of soft tissue
    • Kaposi's sarcoma of soft tissues
    • Kaposi's sarcoma of the CNS
    • Kaposi's sarcoma of the gallbladder
    • Kaposi's sarcoma of the prostate
    • Kaposi's sarcoma, lung
    • Kaposi's sarcoma, skin
    • anal Kaposi's sarcoma
    • cardiac Kaposi's sarcoma
    • central nervous system Kaposi's sarcoma
    • conjunctival Kaposi's sarcoma
    • corneal Kaposi's sarcoma
    • cutaneous Kaposi's sarcoma
    • esophageal Kaposi's sarcoma
    • gallbladder Kaposi's sarcoma
    • gastric Kaposi's sarcoma
    • intestinal Kaposi's sarcoma
    • lymph node Kaposi's sarcoma
    • lymphadenopathic Kaposi's sarcoma
    • palate Kaposi's sarcoma
    • penis Kaposi's sarcoma
    • prostate Kaposi's sarcoma
    • pulmonary Kaposi's sarcoma
    • soft tissue Kaposi's sarcoma
Homo sapiens (human)
DOID:2377
  • multiple sclerosis
  • Aliases:
    • Generalized multiple sclerosis
    • insular sclerosis
Mus musculus (house mouse)
DOID:0111235
  • congenital muscular dystrophy-dystroglycanopathy type A12
  • Aliases:
    • MDDGA12
    • Walker-Warburg syndrome or muscle-eye-brain disease POMK-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A12
Homo sapiens (human)
DOID:0060407
  • chromosome 18q deletion syndrome
  • Aliases:
    • 18q- syndrome
    • deletion 18q
    • monosomy 18q
Homo sapiens (human)
DOID:0070265
  • congenital disorder of glycosylation type IIm
  • Aliases:
    • SLC35A2-CDG
    • congenital disorder of glycosylation type 2m
    • developmental and epileptic encephalopathy 22
    • epileptic encephalopathy, early infantile, 22
Drosophila melanogaster (fruit fly)
DOID:3596
  • placental site trophoblastic tumor
  • Aliases:
    • Placental-Site Gestational Trophoblastic neoplasm
    • placental site trophoblastic tumour
Homo sapiens (human)
DOID:10763
  • hypertension
  • Aliases:
    • HTN
    • hyperpiesia
    • vascular hypertensive disorder
Danio rerio (zebrafish)
DOID:0080109
  • infantile myofibromatosis
  • Aliases:
    • lipofibromatosis
Drosophila melanogaster (fruit fly)
DOID:0080561
  • congenital disorder of glycosylation Ii
  • Aliases:
    • congenital disorder of glycosylation 1i
Saccharomyces cerevisiae S288C
DOID:13399
  • color blindness
  • Aliases:
    • BLINDNESS COLOR
    • Colour blindness
    • Colour vision deficiency
Homo sapiens (human)
DOID:0110521
  • autosomal recessive nonsyndromic deafness 70
  • Aliases:
    • DFNB70
    • autosomal recessive deafness 70
Homo sapiens (human)
DOID:2738
  • pseudoxanthoma elasticum
  • Aliases:
    • Gronblad-Strandberg syndrome
Xenopus laevis (African clawed frog)
DOID:0110163
  • Charcot-Marie-Tooth disease axonal type 2F
  • Aliases:
    • CMT2F
    • Charcot-Marie-Tooth neuronal type 2F
    • Charcot-Marie-Tooth neuropathy type 2F
    • autosomal dominant Charcot-Marie-Tooth disease type 2F
Homo sapiens (human)

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Last updated: August 19, 2024